William W. Hauswirth, PhD
Affiliations: | Ophthalmology | University of Florida, Gainesville, Gainesville, FL, United States |
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"William Hauswirth"Children
Sign in to add trainee| Brian Raisler | grad student | 2003 | UF Gainesville |
| Jason J. Fritz | grad student | 2004 | UF Gainesville |
| Shannon E. Boye | post-doc | UF Gainesville |
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Publications
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| Araujo VG, Dias MS, Hauswirth WW, et al. (2023) rAAV-compatible human mini promoters enhance transgene expression in rat retinal ganglion cells. Experimental Eye Research. 239: 109758 |
| Yan B, Viswanathan S, Brodie SE, et al. (2023) A clinically viable approach to restoring visual function using optogenetic gene therapy. Molecular Therapy. Methods & Clinical Development. 29: 406-417 |
| Occelli LM, Zobel L, Stoddard J, et al. (2023) Development of a translatable gene augmentation therapy for CNGB1-Retinitis Pigmentosa. Molecular Therapy : the Journal of the American Society of Gene Therapy |
| Liu Y, Eastwood JD, Alba DE, et al. (2022) Gene therapy restores mitochondrial function and protects retinal ganglion cells in optic neuropathy induced by a mito-targeted mutant ND1 gene. Gene Therapy |
| Lani-Louzada R, Marra C, Dias MS, et al. (2022) Neuroprotective Gene Therapy by Overexpression of the Transcription Factor MAX in Rat Models of Glaucomatous Neurodegeneration. Investigative Ophthalmology & Visual Science. 63: 5 |
| Aguirre GD, Cideciyan AV, Dufour VL, et al. (2021) Gene therapy reforms photoreceptor structure and restores vision in NPHP5-associated Leber congenital amaurosis. Molecular Therapy : the Journal of the American Society of Gene Therapy |
| Zhu P, Dyka F, Ma X, et al. (2021) Disease mechanisms of X-linked cone dystrophy caused by missense mutations in the red and green cone opsins. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. 35: e21927 |
| Visuvanathan S, Baker AN, Lagali PS, et al. (2021) XIAP gene therapy effects on retinal ganglion cell structure and function in a mouse model of glaucoma. Gene Therapy |
| Aguirre GD, Cideciyan AV, Dufour VL, et al. (2021) Gene Therapy Reforms Photoreceptor Structure and Restores Vision in NPHP5-associated Leber Congenital Amaurosis. Molecular Therapy : the Journal of the American Society of Gene Therapy |
| Wassmer SJ, De Repentigny Y, Sheppard D, et al. (2020) XIAP Protects Retinal Ganglion Cells in the Mutant ND4 Mouse Model of Leber Hereditary Optic Neuropathy. Investigative Ophthalmology & Visual Science. 61: 49 |